| 1 | A functional ABCA1 gene variant is associated with low HDL-cholesterol levels and shows evidence of positive selection in Native Americans | Coautor: Ramírez-Jiménez S., Acuna-Alonzo, V, Flores-Dorantes T., Kruit J.K., et al. | 2010 | HUMAN MOLECULAR GENETICS | WoS-id: 000279469100012
Scopus-id: 2-s2.0-77954145711
| 106 | 115 |
| 2 | Galanin Preproprotein Is Associated With Elevated Plasma Triglycerides | Coautor: Ramírez-Jiménez S., Plaisier C.L., Kyttala, M, Weissglas-Volkov D., et al. | 2009 | ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY | WoS-id: 000261797200024
Scopus-id: 2-s2.0-58849095360
| 24 | 24 |
| 3 | A novel ARH splice site mutation in a Mexican kindred with autosomal recessive hypercholesterolemia | Coautor: Ramírez-Jimenez S., Canizales-Quinteros S., Aguilar-Salinas C.A., Huertas-Vázquez A., et al. | 2005 | HUMAN GENETICS | WoS-id: 000226552200014
Scopus-id: 2-s2.0-19944430011
| 16 | 16 |
| 4 | Mutations in MODY genes are not common cause of early-onset type 2 diabetes in Mexican families | Coautor: Ramírez-Jiménez S., Domínguez-López A., Miliar-García Á., Segura-Kato Y.X., et al. | 2005 | Journal of the Pancreas | Scopus-id: 2-s2.0-27644491272
| 0 | 22 |
| 5 | Identifying different susceptibility loci associated with early onset diabetes and cardiovascular disease in Mexican families [Identificación de distintos loci de susceptibilidad relacionados al desarrollo de diabetes de inicio temprano y e | Coautor: Ramírez-Jiménez S., Canizales-Quinteros S., Huertas-Vázquez A., Riba-Ramírez L., et al. | 2005 | GACETA MEDICA DE MEXICO | Scopus-id: 2-s2.0-20944438524
| 0 | 2 |
| 6 | Association of the calpain-10 gene with type 2 diabetes mellitus in a Mexican population | Coautor: Ramírez-Jiménez S., Del Bosque-Plata L., Aguilar-Salinas C.A., Tusié-Luna M.T., et al. | 2004 | MOLECULAR GENETICS AND METABOLISM | WoS-id: 000188718400007
Scopus-id: 2-s2.0-0347931740
| 39 | 45 |
| 7 | Contribution of chromosome 1q21-q23 to familial combined hyperlipidemia in Mexican families | Coautor: Ramírez-Jiménez S., Huertas-Vázquez A., del Rincón J.P., Canizales-Quinteros S., et al. | 2004 | ANNALS OF HUMAN GENETICS | Scopus-id: 2-s2.0-6444229534
| 16 | 25 |
| 8 | Locus on chromosome 6p linked to elevated HDL cholesterol serum levels and to protection against premature atherosclerosis in a kindred with familial hypercholesterolemia | Coautor: Ramírez-Jiménez S., Canizales-Quinteros S., Aguilar-Salinas C.A., Reyes-Rodríguez E., et al. | 2003 | CIRCULATION RESEARCH | WoS-id: 000181711300015
Scopus-id: 2-s2.0-0037459359
| 29 | 32 |
| 9 | Steroid 21-hydroxylase (P450c21) naturally occuring mutants I172N, v281L and I236N/V237E/M239K exert a dominant negative effect on enzymatic activity when co-expressed with the wild-type protein | Coautor: Ramírez-Jiménez S., Félix-López X., Riba L., Ordóñez-Sánchez Ma.L., et al. | 2003 | JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM | WoS-id: 000185343000010
Scopus-id: 2-s2.0-0141891454
| 5 | 6 |
| 10 | Early-onset type 2 diabetes: Metabolic and genetic characterization in the Mexican population | Coautor: Ramírez-Jiménez S., Aguilar-Salinas C.A., Reyes-Rodríguez E., Ordóñez-Sánchez Ma.L., et al. | 2001 | JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM | WoS-id: 000166580100037
Scopus-id: 2-s2.0-17744369249
| 47 | 52 |
| 11 | Molecular genetic analysis of patients carrying steroid 21-hydroxylase deficiency in the Mexican population: Identification of possible new mutations and high prevalence of apparent germ-line mutations | 2ᵒ autor: Ramírez-Jiménez S., Ordoñez-Sánchez M.L., López-Gutierrez A.U., Riba L., et al. | 1998 | HUMAN GENETICS | WoS-id: 000072457500008
Scopus-id: 2-s2.0-2642651108
| 52 | 59 |
| 12 | Uniparental disomy for chromosome 6 results in steroid 21-hydroxylase deficiency: Evidence of different genetic mechanisms involved in the production of the disease | Coautor: Ramirez-Jiménez S., López-Gutiérrez A.U., Riba L., Ordoñez-Sánchez M.L., et al. | 1998 | JOURNAL OF MEDICAL GENETICS | WoS-id: 000077266400010
Scopus-id: 2-s2.0-0031759339
| 23 | 28 |
| 13 | Analysis of the glucokinase gene in Mexican families displaying early- onset non-insulin-dependent diabetes mellitus including MODY families | Coautor: Ramirez-Jimenez S., Del Bosque-Plata L., Garcia-Garcia E., Cabello-Villegas J., et al. | 1997 | AM J MED GENET | WoS-id: A1997YD48100003
Scopus-id: 2-s2.0-0030735219
| 6 | 7 |
| 14 | Low frequency of deletion alleles in patients with steroid 21-hydroxylase deficiency in a Mexican population | 2ᵒ autor: Ramírez-Jiménez S., Tusié-Luna Ma.T., Ordóñez-Sánchez Ma.L., Cabello-Villegas J., et al. | 1996 | HUMAN GENETICS | Scopus-id: 2-s2.0-0342795410
| 14 | 16 |
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